HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanogen Bromide → HCID 13392479, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | Benalfocin | HCID 123981 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 13392479 | HCID 13392479 | — |
Reaction Steps
A stirred solution of 1.2 g. of 6-chloro-3-methyl-2,3,4,5-tetrahydro-1H-3-benzazepine in 30 ml. of toluene was treated at 50° by dropwise addition with a solution of 0.7 g. cyanogen bromide in 25 ml. of toluene. Following the addition, the mixture was stirred and heated at 50° for one hour. A stream of nitrogen was passed over the surface of the solution during the reaction. The mixture was cooled, filtered and the filtrate concentrated in vacuo to yield 6-chloro-3-cyano-2,3,4,5-tetrahydro-1H-3-benzazepine melting at 81°-82° from hexane-ether solution.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04496558 |
| Source dataset | uspto-grants-1985_01 |
| ORD ID | ord-a4c454f5a33a4e32af9e5bf54f8064ad |
| Source note | uspto-grants-1985_01 |